K261315
- 510(k) number
- K261315
- Device name
- Symbia Pro.specta Q3 (11364751);Symbia Pro.specta X3 (11364752);Symbia Pro.specta X7 (11364753);Symbia Pro.specta VA40 Family
- Applicant
- Siemens Medical Solutions USA, Inc. TN · US
- Product code
- KPS — System, Tomography, Computed, Emission
- Decision date
- 2026-05-21
- Date received
- 2026-04-21
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K261315.pdf
Official FDA record: K261315
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.